Abstract
The novel 3-methyl-2,6-dip-toylpiperidine-4-one was acylated by 3-chloropropanoychloride and subjected for dehydrohalogenation. The synthesized compound was characterized by spectroscopic techniques and finally confirmed by X-ray diffraction studies. The molecule crystallizes in the monoclinic crystal class in the space group C(2)/c with cell parameters a = 18.538(2) angstrom, b = 9.9050(1) angstrom, c = 22.954(2) angstrom, beta = 94.486(8)degrees and Z = 8. The piperidine ring adopts a twist boat conformation.
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